← Back to catalogue

G17 Rapid Quantitative Test (Chemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref BT0505202

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
G17 Rapid Quantitative Test (Chemiluminescence Immunoassay) EUDAMED
Device Name
G17 Rapid Quantitative Test (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
BT0505202 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260206889 EUDAMED
Basic UDI-DI
B-06933260206889 EUDAMED
EMDN Code
W0102039099 TUMOUR MARKERS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Category: Preferentially expressed antigen in melanoma (PRAME) IVD, antibody

G17 Rapid Quantitative Test (Chemiluminescence Immunoassay) by Xiamen Biotime Biotechnology Co., Ltd. — Class IVD General — CE/MDR — listed in EUDAMED

Similar devices

Also classified as Preferentially expressed antigen in melanoma (PRAME) IVD, antibody.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000012852
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED 96649f5e-98c2-4252-a3b1-f360aa9e00eb 61 fields · synced Oct 7, 2026
  • EUDAMED 4f64c25f-1e16-47bd-8647-6509965364dc 61 fields · synced Jul 15, 2026